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Spanish Association of Paediatrics
Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia
Recomendaciones para el diagnóstico y tratamiento de pacientes con formas clásicas de hiperplasia suprarrenal congénita por déficit de 21-hidroxilasa
Amparo Rodrígueza,
Corresponding author
amparorodriguezsanchez@yahoo.es

Corresponding author.
, Begoña Ezquietab, José Igancio Labartac, María Clemented, Rafael Espinoe, Amaia Rodriguezf, Aranzazu Escribanog, In representation of the group of Hiperplasia Suprarrenal Congenita of the Sociedad Española de Endocrinología Pediátrica
a Hospital General Universitario Gregorio Marañón, Madrid, Spain
b Fundación para Investigación Gregorio Marañón, Madrid, Spain
c Hospital Universitario Miguel Servet, Zaragoza, Spain
d Hospital Vall d’Hebron, Barcelona, Spain
e Hospital Universitario Valme, Sevilla, Spain
f Hospital Universitario de Cruces, Barakaldo, Spain
g Hospital Clínico Universitario Virgen Arrixaca, Murcia, Spain
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ISSN: 23412879
Original language: English
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2020 March 342 50 10 402
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